Skip to content

Effects of low-dose aspirin taken at bedtime on pathophysiologic mechanisms underlying hypertension in subjects with grade 1 essential hypertension: the Aspirin In Reduction of Tension (ASPIRETENSION) study - ASPIRETENSION

Effects of low-dose aspirin taken at bedtime on pathophysiologic mechanisms underlying hypertension in subjects with grade 1 essential hypertension: the Aspirin In Reduction of Tension (ASPIRETENSION) study - ASPIRETENSION

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2006-001359-36-NL
Enrollment
15
Registered
2006-03-29
Start date
2006-06-02
Completion date
Unknown
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients should have grade 1 essential hypertension (140/90-159/99 mmHg), but free of history of any cardiovascular events, diabetes mellitus type 1 or 2 or rheumatoid arthritis.

Interventions

Trade Name: Ascal(r) / carbasalate calcium Pharmaceutical Form: Oral powder Pharmaceutical form of the placebo: Oral powder Route of administration of the placebo: Oral use

Sponsors

Leiden University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Essential hypertension, without treatment =65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: -Moderate or severe hypertension (>160/100) -Secondary hypertension -Personal history of cardiovascular events -Diabetes mellitus -Rheumatoid arthritis -Vasoactive medication -Any contraindication to use of aspirin

Design outcomes

Primary

MeasureTime frame
Primary end point(s): -RAAS-activity represented by renin activity;Main Objective: To examine the effects of 100mg aspirin taken at bedtime on plasma renin activity in patients with grade 1 essential hypertension in primary prevention setting.;Secondary Objective: To examine the effects of 100mg aspirin taken at bedtime on (1) other determinants of RAAS-activity, (2) determinants of autonomous nervous activity and (3) determinants of COX-1 and COX-2 mediated activity as well as endothelial inflammation markers, in patients with grade 1 essential hypertension in primary prevention setting

Countries

Netherlands

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026